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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C8B
(R428* +2 more)
Single nucleotide variant
(nonsense)
Complement component 6 deficiency
+2 more
GPathogenic
C6
Microsatellite
(frameshift variant)
Complement component 6 deficiency
+1 more
GPathogenic/Likely pathogenic